CC0 PUBLIC RECORD GRAPH Every score & timeline item links directly to its underlying U.S. FDA record (openFDA, ORA FOIA Reading Room, DECRS & OASIS).
FG
GMPGraphv2.0
Global FDA Facility Graph & Co-Packer Intelligence
Facility Graph → Food & Beverage → Jettal Foods & Specialty Co-Packing
INDEXABLE (PASSES DATA-SUFFICIENCY GATE)
Ownership & Independence Disclosure Disclosure: Jettal is a TDA-registered food manufacturing plant affiliated with GMPGraph founder Perry Belcher. Its FDA Record Index is computed using the identical public formula applied to every facility.
Food & Beverage FEI: 3019482715 DUNS: 117492018 🛡️ LEVEL 4 · MULTI-CYCLE AUDITED CLEAN (GOLD SHIELD)

Jettal Foods & Specialty Co-Packing

Registered Address: Industrial Blvd, Dallas-Fort Worth Metro, TX 75050 (United States)

For Brand Buyers: Jettal Foods & Specialty Co-Packing ranks in the top tier (AAA · 99/100) of Food & Beverage establishments with LEVEL 4 · MULTI-CYCLE AUDITED CLEAN (GOLD SHIELD). Standard quality agreement and lot-by-lot CofA verification apply.
Connected FDA Sources (1): GMPGraph Verified Co-Packer Registry & Inspection Link · Resolved Name Aliases: Jettal Foods & Specialty Co-Packing
AAA
99/100
Clean Record
7-Dim FDA Record Index v2.0
Fewer FDA citations than 99% of tracked Food & Beverage facilities.
Based strictly on public U.S. FDA records as of 2026-11-03. See Formula v2.0
Dim 1 · Credit Grade
AAA (99/100)
Recency-Weighted Index
Dim 2 · Inspection Shield
Level 4 / 4
Consecutive Clean Physical FDA Inspections (NAI)
Dim 4 · 'Elsa' Audit Odds
22%
LOW IMMEDIATE AUDIT PROBABILITY (Routine Cycle)
Dim 5 · 180d WL Escalation
4%
483 → Warning Letter Risk
Dim 6 · Brand Contagion
24 Brands
~99 Downstream SKUs
VERIFIED CONTRACT MANUFACTURER / CO-PACKER AI MOCK-INSPECTION READINESS BADGE

Co-Packing Capabilities, Minimums & Certifications

Request Quote from Jettal Foods & Specialty Co-Packing →

Emerging D2C food, functional culinary, spice/blend, and specialty shelf-stable brands seeking low-MOQ Texas manufacturing.

Minimum Run (MOQ)2,500 units
Typical Turnaround4–6 weeks
In-House Analytical LabYes (FTIR/HPLC/Micro)
Turnkey R&D FormulationAvailable
Dosage & Product Formats:
Dry Food Blends & Functional MixesFermented & Shelf-Stable Culinary ProductsSauces, Rubs & CondimentsPouches & Retail Jars
Registrations & Quality Certifications:
TDA Registered Food Plant21 CFR Part 117 FSMA Preventive ControlsHACCP CertifiedcGMP
LAYER 4 · AI BUYER DUE-DILIGENCE INTERVIEW SCRIPT Tailored to FEI 3019482715's FDA Record

5 Questions to Ask Jettal Foods & Specialty Co-Packing Before Signing a Manufacturing Contract

Bring these exact questions to your discovery call with their QA Director or account rep before wiring a production deposit:

  1. Q1: Do you perform 100% FTIR/HPLC identity testing on incoming active ingredients in-house (21 CFR 111.75(a)(1)), or do you rely on vendor COAs?
  2. Q2: Will you sign our Quality Agreement Rider requiring 24-hour notification if an FDA investigator issues a Form 482 or Form 483 at FEI 3019482715?
  3. Q3: Can we review a redacted Master Manufacturing Record (MMR) and Batch Production Record (BPR) with dual-operator weight verification and yield reconciliation?
  4. Q4: What is your current quarantined finished-product release turnaround for USP microbial limits (<2021>/<2022>) and heavy metals (<2232>)?

Cross-Database Regulatory & Inspection Timeline

Unified chronological history across FDA ORA Inspections, Form 483s, Warning Letters, Enforcement Recalls, and OASIS Import Refusals.

FDA Inspection Classification: NAI · 2026-05-19
Project Area: Food & Beverage · Lead Investigator: Marcus V. Delgado
FDA Inspection Classification: NAI · 2024-10-03
Project Area: Food & Beverage · Lead Investigator: Marcus V. Delgado

Manufacturer Right-of-Reply & Free Match Correction

GUARDRAIL PROTECTED

To ensure fairness and accuracy, facility owners may submit verified Form 483 closeout evidence, CAPA completion statements, or entity-resolution corrections free of charge. Sponsorship never alters an FDA Record Index score.

Dimension 3 · FDA 6-System Model

6-Subsystem cGMP Radar Breakdown

Sub-scores mapped across FDA's six core inspection subsystems.

Quality System (CAPA & OOS) 99/100
Materials & Incoming Identity 99/100
Production & Batch Records 99/100
Facilities, Sanitation & Pest 99/100
Laboratory & Stability Controls 99/100
Packaging & Allergen Labeling 99/100
Layer 6 · Clean-Record Sourcing Alternatives

Verified AAA/AA Co-Packers in This Sector

Compare or request quotes from top-rated contract manufacturers with clean FDA inspection histories:

Score Provenance Receipts

Every point in this facility's FDA Record Index (99/100) is backed by a linked government record (36-month half-life decay).

Event Date Weight Receipt
Clean Inspection (NAI) 2026-05-19 +4.5 pts INSP-3019482715-20260519 ↗
Clean Inspection (NAI) 2024-10-03 +3.1 pts INSP-3019482715-20241003 ↗